Package 67091-137-50

Brand: acetaminophen pm extra strength

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67091-137-50
Digits Only 6709113750
Product NDC 67091-137
Product ID 67091-137_1cd2d784-de45-3a41-e063-6394a90aabdf
Description

1 BOTTLE, PLASTIC in 1 CARTON (67091-137-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2014-12-15
Brand acetaminophen pm extra strength
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Acetaminophen PM Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cd2d784-de45-3a41-e063-6394a90aabdf", "openfda": {"upc": ["0070552230354"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3c57498c-86b0-4ba3-881e-c742a2e8ece5"], "manufacturer_name": ["WinCo Foods, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67091-137-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "67091-137-50", "marketing_start_date": "20141215"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "67091-137_1cd2d784-de45-3a41-e063-6394a90aabdf", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67091-137", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "WinCo Foods, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141215", "listing_expiration_date": "20261231"}